The Duchenne Dystrophy Story: From Phenotype to Gene and Potential Treatment-Reference-Cited by-同舟云学术

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The Duchenne Dystrophy Story: From Phenotype to Gene and Potential Treatment

Published:1989-10 Issue:4 Volume:4 Page:240-250
ISSN:0883-0738
Container-title:Journal of Child Neurology
language:en
Short-container-title:J Child Neurol

Author:

Dubowitz Victor¹

Affiliation:

1. Department of Paediatrics & Neonatal Medicine and the Jerry Lewis Muscle Research Centre, Royal Postgraduate Medical School, Hammersmith Hospital, London, England

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/088307388900400402

Reference73 articles.

Cited by 24 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Drug development progress in duchenne muscular dystrophy;Frontiers in Pharmacology;2022-07-22

2. Pharmacology and toxicology of eteplirsen and SRP-5051 for DMD exon 51 skipping: an update;Archives of Toxicology;2021-11-19

3. Restoring Protein Expression in Neuromuscular Conditions: A Review Assessing the Current State of Exon Skipping/Inclusion and Gene Therapies for Duchenne Muscular Dystrophy and Spinal Muscular Atrophy;BioDrugs;2021-06-07

4. Developing DMD therapeutics: a review of the effectiveness of small molecules, stop-codon readthrough, dystrophin gene replacement, and exon-skipping therapies;Expert Opinion on Investigational Drugs;2021-01-06

5. References;Child Neurology;2021

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